US5985293A - Antioxidative dermocosmetic compositions comprising very low dosages of melatonin/analogs - Google Patents
Antioxidative dermocosmetic compositions comprising very low dosages of melatonin/analogs Download PDFInfo
- Publication number
- US5985293A US5985293A US08/900,109 US90010997A US5985293A US 5985293 A US5985293 A US 5985293A US 90010997 A US90010997 A US 90010997A US 5985293 A US5985293 A US 5985293A
- Authority
- US
- United States
- Prior art keywords
- melatonin
- effective amount
- composition
- dermocosmetic
- appearance
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/4906—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom
- A61K8/4913—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having five membered rings, e.g. pyrrolidone carboxylic acid
- A61K8/492—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having five membered rings, e.g. pyrrolidone carboxylic acid having condensed rings, e.g. indol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/52—Stabilizers
- A61K2800/522—Antioxidants; Radical scavengers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/08—Anti-ageing preparations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q7/00—Preparations for affecting hair growth
Definitions
- the present invention relates to novel dermocosmetic compositions comprising judiciously selected very low dosages of melatonin or analog thereof, having improved antioxidant activity, and which are particularly well-suited for improving or maintaining the appearance of human skin or the scalp.
- Preventing or treating aging of the skin, both intrinsic and extrinsic aging, and the clinical signs described above is essentially a matter of maintaining or improving the appearance of the skin or the scalp.
- Melatonin has also been described for dermocosmetic applications in order to improve the appearance of the skin (JP-61/221,104; WO 86/05093), or to protect the skin against the deleterious effects of irradiation with UV rays (EP-0,438,856; E. Bangha et al., Dermatology, 191, [2], 176 (1995)). It is recommended to use melatonin at concentrations of between 10 -4 and 10% by weight relative to the total weight of the composition.
- WO-86/05093 describes a cosmetic composition comprising melatonin to increase the skin sensitivity towards estrogens, in particular for the treatment of acne or the prevention of hair loss.
- the amounts of melatonin recommended in that application are generally between 10 -4 % and more than 1% by weight relative to the total weight of the composition.
- the only two specific examples of compositions, a lotion for the treatment of acne and a solution for preventing hair loss, comprise 10% and 0.1% by weight of melatonin, respectively.
- EP-438,856 relating to compositions for protection of the skin against the deleterious effects of irradiation with UV rays, recommends amounts of melatonin of between 1% and 10% by weight for topical compositions, the only example of this type of composition comprising 10% melatonin.
- JP-61/221,104 describes a cleansing milk comprising 10% melatonin in order to attenuate skin roughness.
- the antioxidant action of melatonin is not mentioned for the effects studied.
- the present invention features topically applicable dermocosmetic compositions comprising melatonin or analog thereof, at concentrations less than those recommended in the prior art, in order to attain an identical, or even enhanced, antioxidant activity.
- melatonin exhibits no antioxidant activity at a concentration of 10 -5 M, but is active at concentrations less than or equal to 10 -7 M.
- antioxidant activity of hormonal type at the cellular level has also been demonstrated, in particular an activity of inducing the expression of the mRNAs of glutathione peroxidase (GSH), the principal enzyme in the antioxidant defense of the skin, at physiological doses ranging from 10 -9 to 10 -15 M.
- GSH glutathione peroxidase
- the present invention thus features a topical composition
- a topical composition comprising melatonin or analog thereof and a cosmetically or pharmaceutically acceptable support (vehicle, diluent or carrier therefor), in which the amount of melatonin or analog thereof is an amount which is suitable to permit, after topical application and via dermal delivery, the passage of physiological doses of melatonin or analog thereof, of between 10 -15 and 10 -7 M, into the skin.
- the present invention features dermocosmetic compositions comprising melatonin or analog thereof formulated into topically applicable, cosmetically or pharmaceutically acceptable vehicles, diluents or carriers therefor, in which the amount of melatonin or of an analog thereof is strictly less than 10 -4 % by weight relative to the total weight of the composition.
- the amount of melatonin or analog thereof in the compositions according to the invention is preferably less than or equal to 0.5 ⁇ 10 -4 % by weight, more preferably less than or equal to 10 -10 % by weight, advantageously between 10 -12 % and 10 -5 % by weight relative to the total weight of the composition.
- Exemplary melatonin “analogs” include, in particular, its derivatives such as 5-methoxytryptamine, 5-methoxytryptophan, 5-methoxytryptophol, 5-methoxyindole-3-acetic acid and 6-hydroxymelatonin. Also representative are melatoninergic agonists such as those described in WO-95/17405, EP-0,447,285, EP-0,527,687, EP-0,530,087 and EP-0,591,057. These compounds are of natural or synthetic origin.
- compositions of the invention comprising melatonin or analog thereof comprise a cosmetic or dermatological composition and may exist in any pharmaceutical form for topical application which is normal in this art, and the physiologically acceptable vehicle, diluent or carrier may comprise any common support for a cosmetic or dermatological composition.
- compositions may be in the form, in particular, of an aqueous solution or oily suspension or dispersion of the lotion or serum type, emulsions of liquid or semi-liquid consistency of the milk type, obtained by dispersion of a fatty phase in an aqueous phase (O/W) or, conversely, (W/O), or suspensions or emulsions of soft consistency of the cream or aqueous or anhydrous gel type, or, alternatively, microcapsules or microparticles, or vesicule dispersions of ionic and/or nonionic type.
- These compositions are formulated via the usual techniques.
- the amounts of the various constituents of the subject compositions are those conventionally employed in this art.
- compositions in particular, constitute cleansing, protective, treatment or care creams for the face, for the hands, for the feet, for the major anatomical folds or for the body (for example day creams, night creams, makeup-removing creams, foundation creams and antisun/sunscreen creams), fluid foundations, makeup-removing milks, protective or body care milks, antisun/sunscreen milks, skincare lotions, ointments, gels or mousses, such as cleansing lotions, antisun/sunscreen lotions, artificial tanning lotions, compositions for the bath, deodorizing compositions comprising a bactericide, aftershave gels or lotions, hair-removing creams, compositions to prevent insect bites, pain-relief compositions, compositions for treating certain skin diseases such as eczema, rosasea, psoriasis, lichens and severe pruritus.
- cleansing lotions antisun/sunscreen lotions
- artificial tanning lotions compositions for the bath
- the proportion of the fatty phase may range from 5% to 80% by weight, and preferably from 5% to 50% by weight, relative to the total weight of the composition.
- the oils, the waxes, the emulsifiers and the co-emulsifiers formulated into the compositions in emulsion form are selected from among those conventionally employed in the cosmetics art.
- the emulsifier and the co-emulsifier are advantageously present in the composition in a proportion ranging from 0.3% to 30% by weight, and preferably from 0.5 to 20% by weight, relative to the total weight of the composition.
- the emulsifier may, moreover, contain lipid vesicules.
- the fatty phase may represent more than 90% of the total weight of the composition.
- the cosmetic or dermatological composition may also contain additives and adjuvants that are common in the cosmetic or dermatological arts, such as hydrophilic or lipophilic gelling agents, hydrophilic or lipophilic additives, preservatives, antioxidants, solvents, fragrances, fillers, screening agents, odor absorbers and dyestuffs and colorants.
- additives and adjuvants that are common in the cosmetic or dermatological arts, such as hydrophilic or lipophilic gelling agents, hydrophilic or lipophilic additives, preservatives, antioxidants, solvents, fragrances, fillers, screening agents, odor absorbers and dyestuffs and colorants.
- the amounts of these various additives and adjuvants are those conventionally used in these fields and, for example, constitute from 0.01% to 10% of the total weight of the composition.
- these additives and adjuvants may be introduced into the fatty phase, into the aqueous phase, and/or into the lipid spherules.
- oils or waxes include mineral oils (liquid petroleum jelly), plant oils (liquid fraction of karite butter, sunflower oil), animal oils (perhydrosqualene), synthetic oils (Purcellin oil), silicone oils or waxes (cyclomethicone) and fluoro oils (perfluoropolyethers), beeswax, carnauba wax or paraffin wax. Fatty alcohols and fatty acids (stearic acid) may be added to these oils.
- Exemplary emulsifiers include, for example, glyceryl stearate, polysorbate 60 and the mixture of PEG-6/PEG-32/glycol stearate marketed, for example, under the trademark Tefose® 63 by Gattefosse.
- Exemplary solvents include the lower alcohols, in particular ethanol and isopropanol, and propylene glycol.
- hydrophilic gelling agents include carboxyvinyl polymers (carbomer), acrylic copolymers such as acrylate/alkyl acrylate copolymers, polyacrylamides, polysaccharides such as hydroxypropylcellulose, natural gums and clays, and representative lipophilic gelling agents include the modified clays such as bentones, metal salts of fatty acids such as aluminum stearates, hydrophobic silica, ethylcellulose and polyethylene.
- compositions according to the invention may contain other active agents intended, in particular, to prevent and/or treat skin conditions/afflictions.
- compositions according to the invention are particularly well suited for preventing or treating oxidative stress of the skin and/or systems associated therewith, in particular associated with UV irradiation, with aging, with inflammation, with alopecia, etc.
- CM-H2DCF-DA fluorescent probe
- Normal human keratinocytes were incubated for increasing periods (1 h,30 min, 3 h and 6 h) in the presence of melatonin at concentrations ranging from 10 -6 to 10 -17 M.
- the control corresponded to keratinocytes incubated in the absence of melatonin.
- the keratinocytes were taken up in a homogenization buffer.
- the keratinocytes were subjected to three cycles of freezing/thawing, the extract was then centrifuged and the GSH-Px in the supernatant was assayed by the TBH technique described by D. E. Paglia and W. N. Valentine (J. Lab. Clin. Med., 70, 158-169 (1967)).
- Normal human keratinocytes were incubated for increasing periods (1 h,30 min, 3 h and 6 h) in the presence of melatonin at concentrations ranging from 10 -6 to 10 -17 M.
- the control corresponded to keratinocytes incubated in the absence of melatonin.
- the level of expression of GSH-Px was measured after RT-PCR of the mRNA of GSH-Px.
- the level of expression of GSH-Px for each experimental condition was adjusted to that of actin, which represented the internal control.
- Fibroblasts were obtained by the technique of culturing explants. The cells were inoculated in 6-well culture plates.
- the fibroblast culture medium comprised DMEM/M199 medium (3/1 v/v) supplemented with glutamine (2 mM), penicillin (50 IU/ml), streptomycin (50 ⁇ g/ml), sodium bicarbonate (0.2% w/v) and fetal calf serum (10% v/v).
- the fibroblasts were incubated in the FCM medium at 37° C. under a humid atmosphere containing 5% CO 2 , to the stage of confluence of the monolayers. They were incubated in the presence of iron-NTA in order to initiate production of the hydroperoxides which are responsible for a considerable level of radical attack.
- the reference compounds were vitamin E acetate at 1 mg/ml (reference 1) and deferoxamine at 6.5 mg/ml (reference 2).
- CM-H2DCF-DA The melatonin and the reference compounds were dissolved directly in the buffer containing the fluorescent probe at 5 ⁇ M (CM-H2DCF-DA).
- the fibroblasts were incubated with the melatonin or the reference compounds for one hour before the addition of iron-NTA, and then during the incubation in the presence of iron-NTA.
- Control fibroblasts were cultured in the absence of melatonin or reference compounds, in the presence or absence or iron-NTA.
- the fibroblasts were washed by addition of medium and were then lysed by the action of ultrasound.
- the cell lysates were transferred into 96-well plates.
- the probe CM-H2DCF-DA became fluorescent (A. S. Keston and R. Brandt, Anal. Biochem., 11, 1-5 (1965)).
- the fluorescence of the probe was measured by fluorimetry using a plate analyzer (excitation: 355 nm, emission: 460 nm).
- compositions according to the invention illustrate specific compositions according to the invention.
- proportions indicated are percentages by weight.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9609387 | 1996-07-25 | ||
FR9609387A FR2751539B1 (fr) | 1996-07-25 | 1996-07-25 | Nouvelles compositions topiques comprenant de tres faibles doses de melatonine ou ses derives et leur utilisation en cosmetique |
Publications (1)
Publication Number | Publication Date |
---|---|
US5985293A true US5985293A (en) | 1999-11-16 |
Family
ID=9494485
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US08/900,109 Expired - Fee Related US5985293A (en) | 1996-07-25 | 1997-07-25 | Antioxidative dermocosmetic compositions comprising very low dosages of melatonin/analogs |
Country Status (7)
Country | Link |
---|---|
US (1) | US5985293A (es) |
EP (1) | EP0820766B1 (es) |
JP (1) | JP2986432B2 (es) |
CA (1) | CA2210674C (es) |
DE (1) | DE69720613T2 (es) |
ES (1) | ES2196275T3 (es) |
FR (1) | FR2751539B1 (es) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20020183377A1 (en) * | 1999-11-30 | 2002-12-05 | Peter Elsner | Use of melatonin for treating androgenetic and diffuse alopecia |
US20030211126A1 (en) * | 2000-07-13 | 2003-11-13 | Fitzpatrick Richard E | Composition for topically delivering vitamin c |
WO2004039369A1 (de) * | 2002-10-30 | 2004-05-13 | Asat Ag Applied Science & Technology | Melatonin-tagesdosierungseinheiten |
US20040120915A1 (en) * | 2002-12-19 | 2004-06-24 | Kaiyuan Yang | Multifunctional compositions for surface applications |
US20050020666A1 (en) * | 2003-07-25 | 2005-01-27 | Dabur Research Foundation | Cardioprotective agents |
GB2434099A (en) * | 2006-01-12 | 2007-07-18 | Roger Coghill | Very low dosage melatonin compositions and their use in the treatment of the adverse effects of exposure to electromagnetic fields and radiation |
US20090162335A1 (en) * | 2006-03-03 | 2009-06-25 | Mavi Sud S.R.L. | Melatonin and immunostimulating substance-based compositions |
US20100256215A1 (en) * | 2009-04-02 | 2010-10-07 | Silver Eagle Labs Nv, Llc | Menthol-Melatonin Dissolving Film |
US20100256197A1 (en) * | 2009-04-02 | 2010-10-07 | Silver Eagle Labs Nv, Llc | Nicotine Dissolving Film With Or Without Menthol |
US20110236330A1 (en) * | 2008-12-09 | 2011-09-29 | Philippe Moussou | Skin Whitening |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5054945B2 (ja) * | 2006-08-28 | 2012-10-24 | 共栄化学工業株式会社 | 化粧料 |
ES2378028B1 (es) * | 2012-02-22 | 2013-02-18 | Ignacio Umbert Millet | Composición cosmética para el rejuvenecimiento de la piel y procedimiento y usos correspondientes |
WO2019038586A1 (en) | 2017-08-19 | 2019-02-28 | Ftf Pharma Private Limited | PHARMACEUTICAL COMPOSITION OF MELATONIN |
KR102506059B1 (ko) * | 2020-10-20 | 2023-03-07 | 코스맥스 주식회사 | 멜라토닌을 포함하는 항산화용 화장료 조성물 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1986005093A2 (en) * | 1985-03-04 | 1986-09-12 | Cellena (Cell Engineering) A.G. | Melatonin compositions and uses thereof |
WO1987000432A2 (en) * | 1985-07-16 | 1987-01-29 | Cellena (Cell Engineering) A.G. | Use of melatonin or related compounds for the treatment of psoriasis |
US4746674A (en) * | 1985-08-27 | 1988-05-24 | Cellena (Cell Engineering) Ag | Melatonin compositions and uses thereof |
WO1993007870A1 (en) * | 1991-10-18 | 1993-04-29 | Alza Corporation | Device for the transdermal administration of melatonin |
US5560917A (en) * | 1995-02-01 | 1996-10-01 | Maybelline Intermediate Company | Cosmetic makeup composition |
-
1996
- 1996-07-25 FR FR9609387A patent/FR2751539B1/fr not_active Expired - Fee Related
-
1997
- 1997-07-08 DE DE69720613T patent/DE69720613T2/de not_active Expired - Fee Related
- 1997-07-08 EP EP97401632A patent/EP0820766B1/fr not_active Expired - Lifetime
- 1997-07-08 ES ES97401632T patent/ES2196275T3/es not_active Expired - Lifetime
- 1997-07-24 JP JP9199027A patent/JP2986432B2/ja not_active Expired - Fee Related
- 1997-07-24 CA CA002210674A patent/CA2210674C/fr not_active Expired - Fee Related
- 1997-07-25 US US08/900,109 patent/US5985293A/en not_active Expired - Fee Related
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1986005093A2 (en) * | 1985-03-04 | 1986-09-12 | Cellena (Cell Engineering) A.G. | Melatonin compositions and uses thereof |
WO1987000432A2 (en) * | 1985-07-16 | 1987-01-29 | Cellena (Cell Engineering) A.G. | Use of melatonin or related compounds for the treatment of psoriasis |
US4746674A (en) * | 1985-08-27 | 1988-05-24 | Cellena (Cell Engineering) Ag | Melatonin compositions and uses thereof |
WO1993007870A1 (en) * | 1991-10-18 | 1993-04-29 | Alza Corporation | Device for the transdermal administration of melatonin |
US5560917A (en) * | 1995-02-01 | 1996-10-01 | Maybelline Intermediate Company | Cosmetic makeup composition |
Non-Patent Citations (2)
Title |
---|
Reiter, R. J. Interactions of pieal hormone melatonin with oxygen centered free radicals: a brief review, Brazilian J. Med. Res. 26:1141 1155, 1993. * |
Reiter, R. J. Interactions of pieal hormone melatonin with oxygen-centered free radicals: a brief review, Brazilian J. Med. Res. 26:1141-1155, 1993. |
Cited By (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20020183377A1 (en) * | 1999-11-30 | 2002-12-05 | Peter Elsner | Use of melatonin for treating androgenetic and diffuse alopecia |
US20030211126A1 (en) * | 2000-07-13 | 2003-11-13 | Fitzpatrick Richard E | Composition for topically delivering vitamin c |
US20080293803A1 (en) * | 2002-10-30 | 2008-11-27 | Asat Ag Applied Science & Technology | Melatonin daily dosage units |
WO2004039369A1 (de) * | 2002-10-30 | 2004-05-13 | Asat Ag Applied Science & Technology | Melatonin-tagesdosierungseinheiten |
US8062648B2 (en) | 2002-10-30 | 2011-11-22 | Asat Ag Applied Science & Technology | Formulations containing melatonin, ginkgo biloba, and biotin |
US8017645B2 (en) | 2002-10-30 | 2011-09-13 | Asat Ag Applied Science & Technology | Melatonin daily dosage units |
US20060035924A1 (en) * | 2002-10-30 | 2006-02-16 | Asat Ag Applied Science & Technology | Daily melatonin dosing units |
US20060099278A1 (en) * | 2002-10-30 | 2006-05-11 | Asat Ag Applied Science & Technology | Formulations containing melatonin, ginkgo biloba, and biotin |
US20040120915A1 (en) * | 2002-12-19 | 2004-06-24 | Kaiyuan Yang | Multifunctional compositions for surface applications |
US20050020666A1 (en) * | 2003-07-25 | 2005-01-27 | Dabur Research Foundation | Cardioprotective agents |
WO2005009419A3 (en) * | 2003-07-25 | 2005-03-24 | Dabur Res Foundation | Use of 5-methoxytryptamine as a cardioprotective agents |
WO2005009419A2 (en) * | 2003-07-25 | 2005-02-03 | Dabur Research Foundation | Use of 5-methoxytryptamine as a cardioprotective agents |
GB2434099A (en) * | 2006-01-12 | 2007-07-18 | Roger Coghill | Very low dosage melatonin compositions and their use in the treatment of the adverse effects of exposure to electromagnetic fields and radiation |
US20090162335A1 (en) * | 2006-03-03 | 2009-06-25 | Mavi Sud S.R.L. | Melatonin and immunostimulating substance-based compositions |
CN101431997B (zh) * | 2006-03-03 | 2013-01-09 | 马威苏德公司 | 基于褪黑素和免疫抑制物质的组合成分 |
US8802117B2 (en) | 2006-03-03 | 2014-08-12 | Mavi Sud S.R.L. | Melatonin and immunostimulating substance-based compositions |
US20110236330A1 (en) * | 2008-12-09 | 2011-09-29 | Philippe Moussou | Skin Whitening |
US20100256215A1 (en) * | 2009-04-02 | 2010-10-07 | Silver Eagle Labs Nv, Llc | Menthol-Melatonin Dissolving Film |
US20100256197A1 (en) * | 2009-04-02 | 2010-10-07 | Silver Eagle Labs Nv, Llc | Nicotine Dissolving Film With Or Without Menthol |
Also Published As
Publication number | Publication date |
---|---|
EP0820766A2 (fr) | 1998-01-28 |
FR2751539A1 (fr) | 1998-01-30 |
DE69720613T2 (de) | 2004-03-25 |
JPH1067648A (ja) | 1998-03-10 |
EP0820766A3 (fr) | 1998-02-04 |
EP0820766B1 (fr) | 2003-04-09 |
ES2196275T3 (es) | 2003-12-16 |
CA2210674A1 (fr) | 1998-01-25 |
DE69720613D1 (de) | 2003-05-15 |
JP2986432B2 (ja) | 1999-12-06 |
FR2751539B1 (fr) | 1998-12-04 |
CA2210674C (fr) | 2006-11-14 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US6562355B1 (en) | Comixture of dextran sulfate/escin for treating skin redness/edema and/or sensitive skin | |
US6753000B2 (en) | Hydroxystilbene/ascorbic acid compositions for treating skin afflictions | |
US5733558A (en) | Method for treatment of acne and/or the effects of ageing using HMG-coenzyme A-reductase inhibitor and compositions for performing the same | |
JP2941778B2 (ja) | 微生物培地を備える組成物とその使用 | |
US6054137A (en) | Promoting epidermal renewal with phloroglucinol | |
US6267971B1 (en) | Use of cinnamic acid or of its derivatives in a cosmetic firming composition | |
US5985293A (en) | Antioxidative dermocosmetic compositions comprising very low dosages of melatonin/analogs | |
US6521239B1 (en) | Cosmetic composition containing at least one auxin and its use | |
US20100179200A1 (en) | 2-oxothiazolidine 4-carboxylic acid compounds for promoting desquamation of the skin | |
US20070134183A1 (en) | Aminosulfonic acid compounds for promoting desquamation of the skin | |
US5902805A (en) | Method for treatment of acne and/or the effects of ageing using HMG-coenzyme A-reductase inhibitor and compositions for performing the same | |
EP2694025B1 (en) | Use of ethyl gingerone or derivatives thereof for reducing or delaying the signs of skin ageing | |
US6184252B1 (en) | 2-amino-1,3-alkanediol compositions for inducing/stimulating hair growth and/or retarding hair loss | |
US20020103216A1 (en) | 6-substituted pyrimidine 3-oxides for promoting pigmentation of the skin/hair | |
US5939084A (en) | Aqueous phase dermatological/cosmetic compositions comprising solubilized melatonin values | |
US6660283B2 (en) | Use of cinnamic acid, or of at least one of its derivatives in a cosmetic composition | |
US6093409A (en) | Melatonin derivatives and anti-free-radical dermocosmetics comprised thereof | |
US6177089B1 (en) | Use of at least one sulphonic acid for stimulating renewal and/or epidermal repair and for combatting cutaneous aging and conditions | |
US6264962B1 (en) | Use of cinnamic acid or of at least one of its derivatives in a cosmetic composition | |
US6544533B2 (en) | 10-hydroxy-2-decenoic acid compounds for promoting desquamation/epidermal renewal of the skin and/or combating skin aging | |
JPH1171260A (ja) | γ−リノレン酸からなる酸化ストレス防止剤 | |
JP2000510165A (ja) | 皮膚と体成長部の色素脱失のためのアヤメ科抽出物とのフェノール誘導体の組合せとそれを含有する組成物 | |
US20020041908A1 (en) | Iridacea extracts for stimulating the immune system | |
US5618545A (en) | Skin-cosmetic composition | |
US10688029B1 (en) | Formulation preparation to treat mature skin for restoring moisture and retarding aging process |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AS | Assignment |
Owner name: SOCIETE L'OREAL S.A., FRANCE Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:TACHON, PIERRE;PRUCHE, FRANCIS;GERST, CATHERINE;AND OTHERS;REEL/FRAME:008910/0037;SIGNING DATES FROM 19970825 TO 19970908 |
|
FPAY | Fee payment |
Year of fee payment: 4 |
|
FEPP | Fee payment procedure |
Free format text: PAYOR NUMBER ASSIGNED (ORIGINAL EVENT CODE: ASPN); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY |
|
FPAY | Fee payment |
Year of fee payment: 8 |
|
REMI | Maintenance fee reminder mailed | ||
LAPS | Lapse for failure to pay maintenance fees | ||
STCH | Information on status: patent discontinuation |
Free format text: PATENT EXPIRED DUE TO NONPAYMENT OF MAINTENANCE FEES UNDER 37 CFR 1.362 |
|
FP | Lapsed due to failure to pay maintenance fee |
Effective date: 20111116 |